Arroyo Willow Pollen

UNII

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerAllermed Laboratories, Inc.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 4

ndc11
4964340805
5 mL in 1 VIAL, MULTI-DOSE (49643-408-05)
ndc11
4964340810
10 mL in 1 VIAL, MULTI-DOSE (49643-408-10)
ndc11
4964340830
30 mL in 1 VIAL, MULTI-DOSE (49643-408-30)
ndc11
4964340850
50 mL in 1 VIAL, MULTI-DOSE (49643-408-50)

Annotations

UNII (FDA Substance ID)

808UWJ59FI

SALIX LASIOLEPIS POLLEN

RxCUI 852170

Raw payload (JSON)

{
  "unii": {
    "unii": "808UWJ59FI",
    "rxcui": "852170",
    "inchikey": null,
    "display_name": "SALIX LASIOLEPIS POLLEN",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "CUTANEOUS; INTRADERMAL; SUBCUTANEOUS",
  "productid": "49643-408_36ad1e17-751d-e226-e063-6394a90ab328",
  "productndc": "49643-408",
  "dosage_form": "INJECTION",
  "dea_schedule": null,
  "product_type": "NON-STANDARDIZED ALLERGENIC",
  "substance_name": "SALIX LASIOLEPIS POLLEN",
  "proprietary_name": "Arroyo Willow Pollen",
  "active_ingred_unit": "g/mL",
  "application_number": "BLA102211",
  "marketing_category": "BLA",
  "nonproprietary_name": "Salix lasiolepsis",
  "start_marketing_date": "19740312",
  "active_numerator_strength": ".05"
}

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